NIR1 Rabbit pAb, IRDye 800CW conjugated(bs-8513R-IRDye800CW)-100ul

NIR1 Rabbit pAb, IRDye 800CW c

onjugated(bs-8513R-IRDye800CW)-100ul
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  • ¥2980
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  • bs-8513R-IRDye800CW
  • 2025年09月30日
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      100ul

    产品编号bs-8513R-IRDye800CW
    英文名称NIR1 Rabbit pAb, IRDye 800CW conjugated
    中文名称IRDye 800CW标记的膜相关磷脂转运蛋白抗体
    英文别名membrane-associated 3; CORD5; Membrane associated phosphatidylinositol transfer protein 3; Membrane-associated phosphatidylinositol transfer protein 3; NIR 1; NIR-1; NIR1; Phosphatidylinositol transfer protein; Phosphatidylinositol transfer protein, membrane-associated 3; PITM3_HUMAN; PITPnm 3; PITPNM; PITPNM family member 3; Pitpnm3; PYK2 N terminal domain interacting receptor 1; PYK2 N-terminal domain-interacting receptor 1; RDGBA3; retinal degeneration B alpha 3.
    产品应用WB=1000-10000

    Not yet tested in other applications.
    Optimal working dilutions must be determined by the end user.

    抗体来源Rabbit
    免疫原KLH conjugated synthetic peptide derived from human NIR1/RDGBA3
    亚型IgG
    纯化方法affinity purified by Protein A
    克隆类型Polyclonal
    浓度1mg/ml
    储存液0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
    研究领域

    Neuroscience > Neurotransmission > Calcium Signaling > Calcium Channels > IP3R

    Signal Transduction > Protein Phosphorylation > Tyrosine Kinases > Receptor Tyrosine Kinases

    Signal Transduction > Signaling Pathway > Calcium Signaling > Calcium Binding Proteins

    亚基 Interacts with PTK2B via its C-terminus.
    亚细胞定位Endomembrane system; Peripheral membrane protein
    组织特异性Detected in brain and spleen, and at low levels in ovary.
    相似性Belongs to the PtdIns transfer protein family. PI transfer class IIA subfamily.
    Contains 1 DDHD domain. _x000D_
    功能Catalyzes the transfer of phosphatidylinositol and phosphatidylcholine between membranes (in vitro). Binds calcium ions.
    保存条件Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    背景资料Catalyzes the transfer of phosphatidylinositol and phosphatidylcholine between membranes (in vitro) (By similarity). Binds calcium ions.Involvement in disease:Defects in PITPNM3 are the cause of cone-rod dystrophy type 5 (CORD5) . CORDs are inherited retinal dystrophies belonging to the group of pigmentary retinopathies. CORDs are characterized by retinal pigment deposits visible on fundus examination, predominantly in the macular region, and initial loss of cone photoreceptors followed by rod degeneration.

     

    应用推荐稀释比例
    {WB}{1000-10000}

     

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